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1 tosis that led to an enhancement of the slow secretory phase.
2 ies of the functional endometrium during the secretory phase.
3 degeneration shortly after completion of the secretory phase.
5 synthesized by endometrial cells in the late secretory phase and early pregnancy under hormonal regul
7 ated degradation of p27 compared with normal secretory-phase endometrial tissue (SE) such that 4% and
8 an cells that phenocopy murine CD122+Macs in secretory phase endometrium during the implantation wind
11 ive phase and negatively correlated with the secretory phase in both tissues, (ii) IFNgamma and IFNal
16 g increased susceptibility to HIV during the secretory phase of the menstrual cycle, the molecular me
19 ta is expressed during the proliferative and secretory phases of the cycle and is restricted to the l
20 d genes (DEGs) between the proliferative and secretory phases of the cycle in the endocervix (adjuste
23 and ectocervix during the proliferative and secretory phases using RNA sequencing to explore potenti
26 flammatory response/cellular movement in the secretory phase were among the top biofunctions and path
27 expression of Dr ligands occurred during the secretory phase, whereas receptors were expressed in the